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Reversed CD4/CD8 ratios of tumor-infiltrating lymphocytes are correlated with the progression of human cervical carcinoma

Authors :
Pao-Ling Torng
Su-Ming Hsu
Rong-Hwa Lin
Su-Cheng Huang
Hong-Nerng Ho
Bor-Ching Sheu
Source :
Cancer. 86:1537-1543
Publication Year :
1999
Publisher :
Wiley, 1999.

Abstract

BACKGROUND To investigate the clinical significance of tumor-infiltrating lymphocytes (TILs) within the tumor milieu of human cervical carcinoma, the authors quantitatively measured and compared the subpopulations of lymphocytes infiltrating the neoplastic cervix. METHODS A total of 30 patients with Stage Ia–IIa cervical carcinoma were enrolled. TILs were isolated from tissue specimens by means of a mechanical dispersal technique, and the immunocyte subsets were quantified with dual-color flow cytometry. Bulky tumor was defined as tumor size >4 cm in greatest dimension according to the 1995 staging of the International Federation of Gynecology and Obstetrics. RESULTS The CD4/CD8 ratios of TILs were reversed in both cervical squamous cell carcinoma (n = 20) and cervical adenocarcinoma (n = 10). The proportion of CD4+ T cells was significantly lower in tumors from patients with lymph node metastasis (n = 8) than in those from patients without lymph node metastasis (n = 22) (24.5 vs. 32.7, P = 0.001), as was the reversed CD4/CD8 ratio (0.50 vs. 0.81, P = 0.001). The proportion of CD4+ T cells was much lower in bulky tumors (n = 5) than in nonbulky tumors (n = 25) (21.4 vs. 32.5, P < 0.001), reflecting in a more strongly reversed CD4/CD8 ratio (0.41 vs. 0.81, P = 0.001). CONCLUSIONS Decreased proportions of tumor-infiltrating CD4+ T cells with reversed CD4/CD8 ratios are highly correlated with rapid tumor growth and lymph node metastasis in cervical carcinoma. The regional immune escape is of prognostic importance with regard to cancer progression. Cancer 1999;86:1537–43. © 1999 American Cancer Society.

Details

ISSN :
10970142 and 0008543X
Volume :
86
Database :
OpenAIRE
Journal :
Cancer
Accession number :
edsair.doi...........acb71455f79349a97ecf14c89378d448
Full Text :
https://doi.org/10.1002/(sici)1097-0142(19991015)86:8<1537::aid-cncr21>3.0.co;2-d